Class II

Medical Device Recall: PORTRAIT COMPUTE AND CORE SERVICES V1.2, Ref# 5700592

GE Medical Systems Information Technologies Inc · July 20, 2026

Reason for Recall

Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured for each patient or care area.

Distribution

US: MI, NY and Australia, Czech Republic, Finland, Germany, Italy, Netherlands, Qatar, Saudi Arabia, Switzerland, United Arab Emirates, United Kingdom.

States Affected

MI, NY

Quantity Affected

4 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3037-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.